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rs387906981

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906981(C;T)
Make rs387906981(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position39268040
GeneWDR19
is asnp
is mentioned by
dbSNPrs387906981
ebirs387906981
HLIrs387906981
Exacrs387906981
Varsomers387906981
Maprs387906981
PheGenIrs387906981
hapmaprs387906981
1000 genomesrs387906981
hgdprs387906981
ensemblrs387906981
gopubmedrs387906981
geneviewrs387906981
scholarrs387906981
googlers387906981
pharmgkbrs387906981
gwascentralrs387906981
openSNPrs387906981
23andMers387906981
23andMe allrs387906981
SNP Nexus

SNPshotrs387906981
SNPdbers387906981
MSV3drs387906981
GWAS Ctlgrs387906981
Max Magnitude0
ClinVar
Risk rs387906981(A,T;A,T)
Alt rs387906981(A,T;A,T)
Reference rs387906981(C;C)
Significance Pathogenic
Disease Cranioectodermal dysplasia 4
Variation info
Gene WDR19
CLNDBN Cranioectodermal dysplasia 4
Reversed 0
HGVS NC_000004.11:g.39269660C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023682.4,